INFECTION AGE STRUCTURED VECTOR BORNE DISEASE MODEL WITH DIRECT TRANSMISSION.

Mathematical modeling is a powerful tool to study and analyze the disease dynamics prevalent in the community. This thesis studies the dynamics of two time since infection structured vector borne models with direct transmission. We have included disease induced death rate in the first model to form the second model. The aim of this thesis is to analyze whether these two models have same or different disease dynamics. An explicit expression for the reproduction number denoted by R0 is derived. Dynamical analysis reveals the forward bifurcation in the first model. That is when the threshold value R0 < 1, disease free-equilibrium is stable locally implying that if there is small perturbation of the system, then after some time, the system will return to the disease free equilibrium. When R0 > 1 the unique endemic equilibrium is locally asymptotically stable.
For the second model, analysis of the existence and stability of equilibria reveals the existence of backward bifurcation i.e. where the disease free equilibrium coexists with the endemic equilibrium when the reproduction number R02 is less than unity. This aspect shows that in order to control vector borne disease, it is not sufficient to have reproduction number less than unity although necessary. Thus, the infection can persist in the population even if the reproduction number is less than unity. Numerical simulation is presented to see the bifurcation behaviour in the model. By taking the reproduction number as the bifurcation parameter, we find the system undergoes backward bifurcation at R02 = 1. Thus, the model has backward bifurcation and have two positive endemic equilibrium when R02 < 1 and unique positive endemic equilibrium whenever R02 > 1. Stability analysis shows that disease free equilibrium is locally asymptotically stable when R02 < 1 and unstable when R02 > 1. When R02 < 1, lower endemic equilibrium in backward bifurcation is locally unstable.